Volume 124, Issue 3

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October 2008

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14 articles in this issue

Association of Interleukin-1 gene polymorphisms with central obesity and metabolic syndrome in a coronary heart disease population
Kim W. Carter
Joseph Hung
Lyle J. Palmer
Original Investigation 21 August 2008 Pages: 199 - 206
Genome-wide distribution of ancestry in Mexican Americans
Analabha Basu
Hua Tang
Neil Risch
Original Investigation 28 August 2008 Pages: 207 - 214
Gene structure and mutant alleles of PCDH15: nonsyndromic deafness DFNB23 and type 1 Usher syndrome
Zubair M. Ahmed
Saima Riazuddin
Thomas B. Friedman
Original Investigations 22 August 2008 Pages: 215 - 223
Network-based model weighting to detect multiple loci influencing complex diseases
Wei Pan
Original Investigations 22 August 2008 Pages: 225 - 234
Gender influences monoallelic expression of ATP10A in human brain
Amber Hogart
Katherine A. Patzel
Janine M. LaSalle
Original Investigation 23 August 2008 Pages: 235 - 242
Genetic regulation of amniotic fluid TNF-alpha and soluble TNF receptor concentrations affected by race and preterm birth
Ramkumar Menon
Digna R. Velez
Scott M. Williams
Original Investigation 21 September 2008 Pages: 243 - 253
Sequence variants in the PLEKHH2 region are associated with diabetic nephropathy in the GoKinD study population
Christopher N. Greene
Lisa M. Keong
Patricia W. Mueller
Original Investigation 28 August 2008 Pages: 255 - 262
Association of PARL rs3732581 genetic variant with insulin levels, metabolic syndrome and coronary artery disease
Brenda L. Powell
Steven Wiltshire
John P. Beilby
Original Investigations 30 August 2008 Pages: 263 - 270
Germline BRCA1 mutations predispose to pancreatic adenocarcinoma
Wigdan Al-Sukhni
Heidi Rothenmund
Steven Gallinger
Original Investigation 02 September 2008 Pages: 271 - 278
A germline mutation of the KIF1Bβ gene on 1p36 in a family with neural and nonneural tumors
I-Tien Yeh
Romina E. Lenci
Patricia L. M. Dahia
Original Investigations 26 August 2008 Pages: 279 - 285
LRRK2 R1628P increases risk of Parkinson’s disease: replication evidence
E. K. Tan
Louis C. Tan
Yi Zhao
Short Report 10 September 2008 Pages: 287 - 288
Merlin G. Butler, Philip D. K. Lee, Barbara Y. Whitman: Management of Prader-Willi syndrome
Ruth Newbury-Ecob
Book Review 10 September 2008 Pages: 289 - 290
Jan A. Witkowski and John R. Inglis (eds): Davenport’s dream. Twenty-first century reflections on heredity and eugenics
Ian D. Young
Book Review 25 August 2008 Pages: 291 - 292
Novel human pathological mutations

Human Gene Mutations 12 September 2008 Pages: 293 - 324

Volume 124, Issue 3

Association of Interleukin-1 gene polymorphisms with central obesity and metabolic syndrome in a coronary heart disease population

Genome-wide distribution of ancestry in Mexican Americans

Gene structure and mutant alleles of PCDH15: nonsyndromic deafness DFNB23 and type 1 Usher syndrome

Network-based model weighting to detect multiple loci influencing complex diseases

Gender influences monoallelic expression of ATP10A in human brain

Genetic regulation of amniotic fluid TNF-alpha and soluble TNF receptor concentrations affected by race and preterm birth

Sequence variants in the PLEKHH2 region are associated with diabetic nephropathy in the GoKinD study population

Association of PARL rs3732581 genetic variant with insulin levels, metabolic syndrome and coronary artery disease

Germline BRCA1 mutations predispose to pancreatic adenocarcinoma

A germline mutation of the KIF1Bβ gene on 1p36 in a family with neural and nonneural tumors

LRRK2 R1628P increases risk of Parkinson’s disease: replication evidence

Merlin G. Butler, Philip D. K. Lee, Barbara Y. Whitman: Management of Prader-Willi syndrome

Jan A. Witkowski and John R. Inglis (eds): Davenport’s dream. Twenty-first century reflections on heredity and eugenics

Novel human pathological mutations

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